Process for preparing CHF20CHFCF3 and CHF20CHC1CF3 and novel intermediate compounds employed therein

ABSTRACT

Process for preparing CHF 2  OCHFCF 3  through the use of novel intermediate compounds CHCl 2  OCH 2  COCl and CHCl 2  OCHClCOCl.

This is a division of application Ser. No. 220,129 filed July 18, 1988 now U.S. Pat. No. 4,855,511.

FIELD OF THE INVENTION

The present invention is directed to the field of inhalation anesthetics and particularly to methods of. producing known volatile liquid inhalation anesthetics from inexpensive starting materials.

BACKGROUND OF THE INVENTION

Volatile liquid inhalation anesthestics are known in the art and include by way of example halothane, trichloroethylene, and halogenated ether derivatives including enflurane, fluroxene, methoxyflurane, isoflurane and 2-(difluoromethoxy)-1,1,1,2-tetra-fluoroethane.

The latter two inhalation anesthetics have received much attention because they provide a rapid rate of recovery and therefore are particularly suitable for administering to patients during outpatient surgery.

The most common method of preparing isoflurane (CHF₂ OCHClCF₃) is by the reaction of trifluoroethanol (CF₃ CH₂ OH) and chlorodifluoromethane (CF₂ HCl) in the presence of an organic base to produce a compound of the formula CHF₂ OCH₂ CF₃ which is then reacted with chlorine gas in the presence of light energy and optionally an organic solvent to thereby obtain isoflurane.

2-(difluoromethoxy)-1,1,1,2-tetrafluoroethane (hereinafter referred to as "CHF₂ OCHFCF₃ ") is most commonly produced by reacting isoflurane with a fluorinating agent such as BrF₃. The production of CHF₂ OCHFCF₃ is largely dependent on the starting materials used to prepare isoflurane.

The starting material, trifluoroethanol, is both difficult to produce and expensive to obtain. Use of this starting material therefore significantly increases the cost of producing both isoflurane and CHF₂ OCHFCF₃.

It is therefore an object of the invention to provide methods of producing isoflurane and CHF₂ OCHFCF₃ from inexpensive starting materials.

It is a further object of the invention to employ novel intermediate compounds for the production of isoflurane and CHF₂ OCHFCF₃.

SUMMARY OF THE INVENTION

The present invention is generally directed to a process of preparing a compound of the formula CHF₂ OCHFCF₃ from the novel starting compound dichloromethoxy--α-chloroacetyl chloride (hereinafter referred to as "CHCl₂ OCHClCOCl") and to a process in which both CHF₂ OCHFCF₃ and isoflurane (CHF₂ OCHClCF₃) are produced through the use of inexpensive starting materials and novel intermediates.

DETAILED DESCRIPTION OF THE INVENTION

The process of the present invention comprises reacting the novel compound CHCl₂ OCHClCOCl with SF₄ to produce the anesthetic CHF₂ OCHFCF₃. The reaction is conducted at elevated temperatures, preferably in the range of about 145° to 155° C. Isoflurane is also produced and can be converted by known methods into CHF₂ OCHFCF₃ for retained for use as an anesthetic.

CHCl₂ OCHClCOCl may be prepared by reacting CH₃ OCH₂ COOH with a chlorinating agent such as SOCl₂ or PCl₅ to produce the corresponding acid chloride which in turn is reacted with chlorine gas in the presence of light energy either neat or in an organic solvent such as carbon tetrachloride, to produce CHCl₂ OCH₂ COCl as a first novel intermediate compound and CHCl₂ OCHlCOCl as a second novel intermediate compound.

The yield of the first and second novel intermediates is temperature dependent. In general the reaction may be conducted at a temperature in the range of about -15° C. to the boiling point of the solvent, or in the absence of a solvent, to about 50° C.

An increased yield of the first novel intermediate is favored by lower temperatures in the above described temperature range, preferably about 0° to 15° C., most preferably about 10° C. A higher yield of the first intermediate is desirable for the production of isoflurane (CHF₂ OCHClCF₃).

On the other hand, for the direct production of CHF₂ OCHFCF₃, increasing the yield of the second intermediate is desirable. Accordingly, the reaction of CH₃ OCH₂ COCl and chlorine gas in the presence of light energy is conducted at higher temperatures than 10° C., preferably at least 20° C.

The second intermediate compound may be reacted with SF₄ at elevated temperatures in accordance with the invention to yield the desired compound CHF₂ OCHFCF₃.

The first intermediate compound may be reacted with SF₄ at elevated temperatures to produce the isoflurane precursor CHF₂ OCH₂ CF₃, which in turn is reacted with chlorine gas and light energy, optionally in the presence of an organic solvent, to yield isoflurane. The isoflurane thus produced may be converted to CHF₂ OCHFCF₃ by reaction with a fluorinating agent such as bromine trifluoride.

CHF₂ OCHFCF₃ is normally a clear, colorless, liquid having the following physical properties: boiling point 23.5° C., molecular weight 168, estimated vapor pressure 660 mmHg at 20° C., and a specific gravity of 1.44. IR shows a prominent peak at 4903 cm⁻¹ and the ¹ H NMR shows a triplet at 6.5 ppm (J=70 Hz) and a doublet of quartets at 5.9 ppm (J_(gem) =56 Hz, J_(vic) =3 Hz). The compound is non-flammable, and stable to soda lime, rendering it particularly suitable as an inhalation anesthetic. Other characteristics and descriptions of CHF₂ OCHFCF₃ and anesthetic compositions containing the same are disclosed in U.S. Pat. No. 4,762,856, incorporated herein by reference.

EXAMPLE 1 Production of CHCl₂ OCHClCOCl From Methoxy Acetyl Chloride

18.9 g of methoxy acetyl chloride (CH₃ OCH₂ COCl) and 200 ml of CCl₄ were added to a 300ml reactor fitted with an outer cooling jacket. The temperature of the reactor was maintained at -5° to 5° C. Chlorine gas was gradually added to the reactor through a gas dispersion tube at the rate of 0.002 liter/min (0.057 mg/min).

After approximately 16 hours, the chlorine gas flow was reduced to its lowest visual setting as evidenced by the presence of bubbles in the reaction solution and continued for 8 additional hours. The reaction mass was then warmed to room temperature and the CCl₄ distilled off at ambient pressure. The resulting product (37.6 g) was transferred to a 50 ml flask and vacuum distilled to produce a fraction having the following characteristics:

    bp.sub.52 mm =to 89° C. (10.4 g)

The ¹ H NMR showed a 7.4 ppm singlet for CHCl₂ --O-- and a 4.6 ppm singlet for --O--CH₂ COCl.

EXAMPLE 2 Production of CHCl₂ OCH₂ ClCOCl From Methoxy Acetyl Chloride

20 g of methoxy acetyl chloride and 168 g of CCl₄ were added to the same reactor described in Example 1. The temperature of the reactor was maintained at about 30° C. Chlorine gas was gradually added to the reactor through a gas dispersion tube at approximately the same rate as described in Example 1 over approximately three hours.

The reaction mass was then allowed to warm to room temperature and the CCl₄ was distilled off at ambient pressure. The resulting product was vacuum distilled to produce a fraction having the following characteristics:

    bp.sub.(2.0-4.7 mm)=42°-55° C. (17.2 g)

The ¹ H NMR showed a 7.7 ppm singlet for CHCl₂ --O-- and a 5.9 ppm singlet for --O--CH₂ COCl.

EXAMPLE 3 Reaction of CHCl₂ OCHClCOCl with SF₄

A stainless steel tube reactor containing 6.3 g (0.03 moles) of CHCl₂ OCHClCOCl produced in Example 1 was cooled with liquid nitrogen and 13.3 g (0.06 moles) of SF₄ was condensed into the stainless steel tube reactor. The reactor was warmed to room temperature and then heated to and maintained at a temperature of 145°-155° C. for 6 hours during which time the resulting pressure was from 600-650 psig.

The reactor was then cooled to room temperature and the resulting gaseous products were collected in a scrubber containing a 9% NaOH solution maintained at 10° C. The reactor was then heated to 80° C. and additional distillate collected in the NaOH scrubber. The scrubber was then heated to 100° C. to yield an organic phase which was collected in a Dean-Stark trap cooled to 0° C. Two cuts of 2.9 g and 0.5 g were collected in the trap. The cuts were analyzed by gas chromatography and found to have the following composition:

    ______________________________________                                         Component    Wt (g)      Moles   % Yield                                       ______________________________________                                         CHF.sub.2 OCHFCF.sub.3                                                                      1.44        0.0086  29%                                           isoflurane   1.47        0.0080  27%                                           ______________________________________                                    

EXAMPLE 4 Reaction of CHCl₂ OCH₂ COCl With SF₄

A stainless steel tube reactor containing 10.4 g (0.059 moles) of CHCl₂ OCH₂ COCl produced in Example 2 was cooled with liquid nitrogen and 14.6 g (0.07 moles) of SF₄ was condensed into the tube reactor. The reactor was allowed to warm to room temperature and then gradually warmed to 132° C. over the course of 21/2 hours. The pressure in the reactor increased from 95 to 505 psig.

Thereafter the temperature of the reactor was gradually raised to between 143° to 163° C. for about 1 hour causing the pressure in the reactor to increase to between 585 to 645 psi. The reactor was then maintained at a temperature between 145° to 155° C. for about 4 hours at an autogenous pressure of between 595 to 605 psig.

The reactor was then cooled to room temperature and the resulting gases were vented into a scrubber containing a solution of 50 g of 50% NaOH in 320 g of water at a temperature of -10° C.

The resulting organic layer (8.7 g) was separated from the aqueous phase. Gas chromatography showed a retention time (3.97 min) similar to that of CF₃ CH₂ OCHF₂. The product was separately tested in a mass spectropnotometer and ¹ H NMR and the above structure was confirmed. The yield of the product was 69%. The resulting product can be readily converted to isoflurane (CHF₂ OCHClCF₃) by reaction with chlorine gas in the presence of light energy. 

What we claim is:
 1. A compound of the formula CHCl₂ OCH₂ COCl.
 2. A compound of the formula CHCl₂ OCHClCOCl. 